Effect of Tele-Yoga Therapy on Patients With Chronic Musculoskeletal Pain During Covid-19 Lockdown
- Conditions
- Chronic Musculoskeletal Pain
- Interventions
- Other: Primary careOther: Tele-yoga therapy
- Registration Number
- NCT04466605
- Lead Sponsor
- Aarogyam UK
- Brief Summary
Covid-19 outbreak and lockdown measures raised significant concerns over clinical management of chronic pain patients around the world. Patients with chronic musculoskeletal pain (CMSP) are at high risk of physical disability, psychological distress, and poor quality of life. Analgesic medications were main management during lockdown, but opioid-related concerns have prompted to find immediate alternatives.
Present study was undertaken to determine whether patients randomized to tele-yoga therapy would experience less pain, disability and improved global health, adherence and satisfaction, compared with patients assigned to usual care.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 64
- Patients having pain that was musculoskeletal, defined as regional (joints, limbs, back, neck) or more generalized (fibromyalgia or chronic widespread pain);
- Persistent pain ( ≥3 months) despite trying conventional treatment.
- Access to virtual platform with internet.
- Ready to give informed consent
- Schizophrenia,
- Psychiatric disorder
- Cognitive impairment
- Suicidal ideation
- Current illicit drug use
- Terminal illness
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Usual Care Primary care Patients randomized to usual care continued to receive care for their chronic musculoskeletal pain from their primary care physician. There was no attempt by to influence clinical management unless an emergency arose Tele-Yoga Therapy Tele-yoga therapy All patients randomized to the intervention group had one to one yoga sessions with yoga therapist twice a week for 45 minutes on secure virtual platform. Patients were encouraged with home practice to follow everyday at least for 30-mins.
- Primary Outcome Measures
Name Time Method Interference of pain From baseline to 6-week post intervention Interference of pain in 7 areas (mood, physical activity, work, social activity, relations with others, sleep, enjoyment of life) were reported using BPI
Severity of pain From baseline to 6-week post intervention Pain was assessed using the Brief Pain Inventory (BPI), which rates the severity of pain on 4 items (current, worst, least, and average pain in past week)
- Secondary Outcome Measures
Name Time Method Global rating of change in pain From baseline to 6-week post interventiona 7-point global rating of pain change was used to assess change in pain
Intervention specific satisfaction From baseline to 6-week post interventiona 10 point scale was used to assess intervention-specific satisfaction
Trial Locations
- Locations (1)
NMP Medical Research Institute
🇮🇳Jaipur, Rajasthan, India